Canonical Allele Identifier: CA891317850

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1429021631
• gnomAD v3: 1-173917032-G-T
• gnomAD v4: 1-173917032-G-T
• MyVariant Identifiers: chr1:g.173886170G>T (hg19) ; chr1:g.173917032G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173917032G>T , CM000663.2:g.173917032G>T	GRCh38
NC_000001.10:g.173886170G>T , CM000663.1:g.173886170G>T	GRCh37
NC_000001.9:g.172152793G>T	NCBI36
NG_012462.1:g.5347C>A , LRG_577:g.5347C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.41+187C>A MANE Select	ENSP00000356671.3:n.41+187C>A
ENST00000367698.3:c.41+187C>A	ENSP00000356671.3:n.41+187C>A
ENST00000494024.1:n.98+187C>A
ENST00000617423.4:c.41+187C>A	ENSP00000478688.1:n.41+187C>A
NM_000488.3:c.41+187C>A , LRG_577t1:c.41+187C>A	NP_000479.1:n.41+187C>A
XM_005245198.2:c.-273+187C>A	XP_005245255.1:n.-273+187C>A
NM_001365052.1:c.-273+187C>A	NP_001351981.1:n.-273+187C>A
NM_000488.4:c.41+187C>A MANE Select	NP_000479.1:n.41+187C>A
NM_001365052.2:c.-273+187C>A	NP_001351981.1:n.-273+187C>A
NM_001386302.1:c.41+187C>A	NP_001373231.1:n.41+187C>A
NM_001386303.1:c.24+204C>A	NP_001373232.1:n.24+204C>A
NM_001386304.1:c.41+187C>A	NP_001373233.1:n.41+187C>A
NM_001386305.1:c.41+187C>A	NP_001373234.1:n.41+187C>A
NM_001386306.1:c.41+187C>A	NP_001373235.1:n.41+187C>A